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Updated: Aug 16, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Kennedy's disease phenotype with positive genetic study for Kugelberg-Welander's disease: case report

Ana P Trentin1, Rosana H Scola, Hélio A G Teive

  • 1Department of Internal Medicine, Neuromuscular Service, Clinical Hospital, Universidade Federal do Paraná, Curitiba PR, Brazil.

Arquivos De Neuro-Psiquiatria
|August 17, 2005
PubMed

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